Modulus 6793037P2Recalls & reported problems
Nuvasive, Inc. · Modulus-C, 7x17x14mm 7° · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517941657), received between Jan 14, 2025 and Jan 14, 2025 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Dysphagia/ Odynophagia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE EVENT WAS IDENTIFIED DURING A REVIEW OF THE CERVICAL INTERBODY PMCF STUDY, THE REPORT IDENTIFIED THAT ON (B)(6) 2023 A PATIENT UNDERWENT A TWO LEVEL ANTERIOR CERVICAL DISCECTOMY FUSION PROCEDURE AT C3/4 WITH AN ANTERIOR FIXATION PLATE WHERE THE SURGEON NOTED "LOSS OF AIRWAY DURING SURGERY". ON (B)(6) 2024 PRESENTED WITH DIFFICULTY SWALLOWING AND PRODUCING MUCUS TO SPIT OUT AND REFERRED TO A SPEECH THERAPIST AND CONSIDERED A DYSPHAGIA COMPLICATION.
Patient problems: Dysphagia/ Odynophagia
MAUDE report 21150460 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.